Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g61560 A09 58528350 G A upstream_gene_variant MODIFIER c.-3135G>A| S184
2 BAA09g61560 A09 58528796 C T upstream_gene_variant MODIFIER c.-2689C>T| S183
S198
3 BAA09g61560 A09 58529634 C T upstream_gene_variant MODIFIER c.-1851C>T| S261
4 BAA09g61560 A09 58530794 G A upstream_gene_variant MODIFIER c.-691G>A| S32
5 BAA09g61560 A09 58531093 C T upstream_gene_variant MODIFIER c.-392C>T| S5
6 BAA09g61560 A09 58533705 G A missense_variant MODERATE c.1640G>A|p.Gly547Glu S193
7 BAA09g61560 A09 58534540 C T missense_variant MODERATE c.2135C>T|p.Pro712Leu S34
8 BAA09g61560 A09 58534554 G A missense_variant MODERATE c.2149G>A|p.Glu717Lys S112
9 BAA09g61560 A09 58534578 G A missense_variant MODERATE c.2173G>A|p.Val725Ile S246
10 BAA09g61560 A09 58535265 G A missense_variant MODERATE c.2860G>A|p.Ala954Thr S243
11 BAA09g61560 A09 58535266 C T missense_variant MODERATE c.2861C>T|p.Ala954Val S303
12 BAA09g61560 A09 58535473 C T missense_variant MODERATE c.2986C>T|p.Pro996Ser S275
13 BAA09g61560 A09 58535733 G A splice_region_variant&intron_variant LOW c.3240+6G>A| S193
14 BAA09g61560 A09 58537120 C T downstream_gene_variant MODIFIER c.*635C>T| S82
S92